Template:Heidelberg/project/rd/clickchemistry
Click Chemistry
Hein et al. describe the copper-catalysed azide-alkyne cycloaddition (CuAAC) and the positive aspects of it as well as the importance of using copper as a catalyst
The advantages of a click reaction are that it is very simple and works under many different conditions, as well as that the reaction results in high yields with no byproducts. The highly energetic azides react with alkynes enabling a selective reaction that links reactive groups to one another.
An azide anion is a strong nucleophile that easily substitutes potential leaving groups. Thus, azides react with alkynes via a dipolar cycloaddition. The reaction itself is a highly exothermic one with a ∆H° between -50 and -60 kcal mol-1. However, on the contrary, the activation energy is high too (24-26kcal mol-1
With regard to the choice of catalyst used, copper (Cu(I)) proves to be the most thermodynamically stable one. Hence, the thermal reaction proceeds rapidly into a 1,2,3 triazole heterocycle which provides many positive features. Its aromatic character, strong dipole moment, high chemical stability and capability of accepting hydrogen bonds make it highly applicable for many chemical reactions in a broad field of science
Additionally, ascorbate is added to the reaction as a reductant maintaining the oxidation state of copper. Furthermore, a ligand is important to prevent the unwanted influence of ROS (reactive oxygen species) by protecting the biomolecules from oxidation
Martin et al. have shown that yeast PolyA Polymerase is able to incorporate certain modified NTPs
The transformation of a terminal label into an internal label, one can be achieved by splinted ligation using a DNA template that is complementary to the two RNA templates that are to be connected to each other